메뉴 건너뛰기




Volumn 360, Issue 1-2, 2008, Pages 213-218

Dissolution-rate enhancement of fenofibrate by adsorption onto silica using supercritical carbon dioxide

Author keywords

Adsorption; Dissolution rate enhancement; Fenofibrate; Poorly water soluble drugs; Silica; Supercritical carbon dioxide

Indexed keywords

CARBON DIOXIDE; FENOFIBRATE; SILICON DIOXIDE; SUPERCRITICAL CARBON DIOXIDE;

EID: 47049131872     PISSN: 03785173     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijpharm.2008.04.041     Document Type: Article
Times cited : (99)

References (38)
  • 1
    • 0014136951 scopus 로고
    • Deaggregation behavior of a relatively insoluble substituted benzoic acid and its sodium salt
    • Aguiar A.J., Zelmer A.W., and Kinkel A.W. Deaggregation behavior of a relatively insoluble substituted benzoic acid and its sodium salt. J. Pharm. Sci. 56 (1967) 1243-1252
    • (1967) J. Pharm. Sci. , vol.56 , pp. 1243-1252
    • Aguiar, A.J.1    Zelmer, A.W.2    Kinkel, A.W.3
  • 2
    • 34249755913 scopus 로고
    • Increasing the solubility characteristics of fenofibrate with cyclodextrin
    • Aigner Z., Bencz I., and Kata M. Increasing the solubility characteristics of fenofibrate with cyclodextrin. J. Inclusion Phenomena Mol. Recognit. Chem. 20 (1995) 1-252
    • (1995) J. Inclusion Phenomena Mol. Recognit. Chem. , vol.20 , pp. 1-252
    • Aigner, Z.1    Bencz, I.2    Kata, M.3
  • 3
    • 0028948839 scopus 로고
    • A theoretical basis for a biopharmaceutical drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability
    • Amidon G.L., Lennernas H., Shah V.P., and Crison J.R. A theoretical basis for a biopharmaceutical drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm. Res. 12 (1995) 413-420
    • (1995) Pharm. Res. , vol.12 , pp. 413-420
    • Amidon, G.L.1    Lennernas, H.2    Shah, V.P.3    Crison, J.R.4
  • 4
    • 47049090139 scopus 로고    scopus 로고
    • Cabot Corp., 2007. Applications of CAB-O-SIL M-5P fumed silica in formulation and design of solid dosage forms. Available via www.cabot-corp.com (accessed on June 20, 2007).
    • Cabot Corp., 2007. Applications of CAB-O-SIL M-5P fumed silica in formulation and design of solid dosage forms. Available via www.cabot-corp.com (accessed on June 20, 2007).
  • 5
    • 47049120540 scopus 로고    scopus 로고
    • Cabot Corp., 2007. Functions of CAB-O-SIL fumed silica in pharmaceutical applications. Available via www.cabot-corp.com (accessed on June 20, 2007).
    • Cabot Corp., 2007. Functions of CAB-O-SIL fumed silica in pharmaceutical applications. Available via www.cabot-corp.com (accessed on June 20, 2007).
  • 6
    • 47049084830 scopus 로고    scopus 로고
    • Cabot Corp., 2007. Properties of CAB-O-SIL M-5P fumed silica. Available via www.cabot-corp.com (accessed on June 20, 2007).
    • Cabot Corp., 2007. Properties of CAB-O-SIL M-5P fumed silica. Available via www.cabot-corp.com (accessed on June 20, 2007).
  • 8
    • 0021329149 scopus 로고
    • Amorphous spray-dried hydroflumethiazide-polyvinylpyrrolidone systems: physicochemical properties
    • Corrigan O.I., and Holohan E.M. Amorphous spray-dried hydroflumethiazide-polyvinylpyrrolidone systems: physicochemical properties. J. Pharm. Pharmacol. 36 (1984) 217-221
    • (1984) J. Pharm. Pharmacol. , vol.36 , pp. 217-221
    • Corrigan, O.I.1    Holohan, E.M.2
  • 9
    • 0035073301 scopus 로고    scopus 로고
    • Modeling and comparison of dissolution profiles
    • Costa P., and Lobo J.M.S. Modeling and comparison of dissolution profiles. Eur. J. Pharm Sci. 13 (2001) 123-133
    • (2001) Eur. J. Pharm Sci. , vol.13 , pp. 123-133
    • Costa, P.1    Lobo, J.M.S.2
  • 10
    • 0014318742 scopus 로고
    • Dissolution kinetics of drugs in human gastric juice the role of surface tension
    • Finholt P., and Slovang S. Dissolution kinetics of drugs in human gastric juice the role of surface tension. J. Pharm. Sci. 57 (1968) 1322-1326
    • (1968) J. Pharm. Sci. , vol.57 , pp. 1322-1326
    • Finholt, P.1    Slovang, S.2
  • 11
    • 31344476101 scopus 로고    scopus 로고
    • Dissolution rate improvement of poorly water soluble drugs obtained by adsorbing solutions of drugs in solvents onto high surface area carriers
    • Friedrich H., Fussnegger B., Kolter K., and Bodmeier R. Dissolution rate improvement of poorly water soluble drugs obtained by adsorbing solutions of drugs in solvents onto high surface area carriers. Eur. J. Pharm. Biopharm. 62 (2006) 171-177
    • (2006) Eur. J. Pharm. Biopharm. , vol.62 , pp. 171-177
    • Friedrich, H.1    Fussnegger, B.2    Kolter, K.3    Bodmeier, R.4
  • 12
    • 0035095847 scopus 로고    scopus 로고
    • Characterization of glass solutions of poorly water-soluble drugs produced by melt extrusion with amorphous polymers
    • Froster A., Hempenstall J., and Rades T. Characterization of glass solutions of poorly water-soluble drugs produced by melt extrusion with amorphous polymers. J. Pharm. Pharmacol. 53 (2001) 303-315
    • (2001) J. Pharm. Pharmacol. , vol.53 , pp. 303-315
    • Froster, A.1    Hempenstall, J.2    Rades, T.3
  • 14
    • 0030638567 scopus 로고    scopus 로고
    • Characteristics and significance of the amorphous state in pharmaceutical systems
    • Hancock B.C., and Zorafi G. Characteristics and significance of the amorphous state in pharmaceutical systems. J. Pharm. Sci. 86 (1997) 1-12
    • (1997) J. Pharm. Sci. , vol.86 , pp. 1-12
    • Hancock, B.C.1    Zorafi, G.2
  • 16
    • 33746101876 scopus 로고    scopus 로고
    • Role of surfactant and pH on dissolution properties of fenofibrate and glipizide-technical note
    • Jamzad S., and Fassihi R. Role of surfactant and pH on dissolution properties of fenofibrate and glipizide-technical note. AAPS Pharm. Sci. Tech. 7 (2006) E1-E6
    • (2006) AAPS Pharm. Sci. Tech. , vol.7
    • Jamzad, S.1    Fassihi, R.2
  • 17
    • 47049093806 scopus 로고    scopus 로고
    • Jmol. An open-source java viewer for chemical structures in 3D. Available via http://jmol.sourceforge.net/ (accessed on August 15, 2007).
    • Jmol. An open-source java viewer for chemical structures in 3D. Available via http://jmol.sourceforge.net/ (accessed on August 15, 2007).
  • 19
    • 5144219871 scopus 로고    scopus 로고
    • Amorphous drug delivery systems: molecular aspects, design, and performance
    • Kaushal A.M., Gupta P., and Bansal A.K. Amorphous drug delivery systems: molecular aspects, design, and performance. Crit. Rev. Ther. Drug Carrier Syst. 21 (2004) 133-193
    • (2004) Crit. Rev. Ther. Drug Carrier Syst. , vol.21 , pp. 133-193
    • Kaushal, A.M.1    Gupta, P.2    Bansal, A.K.3
  • 21
    • 0029080002 scopus 로고
    • Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: absolute oral bioavailability of nanocrystalline danzol in beagle dogs
    • Liversidge G.G., and Cundy K.C. Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: absolute oral bioavailability of nanocrystalline danzol in beagle dogs. Int. J. Pharm. 125 (1995) 91-97
    • (1995) Int. J. Pharm. , vol.125 , pp. 91-97
    • Liversidge, G.G.1    Cundy, K.C.2
  • 22
    • 34247529516 scopus 로고    scopus 로고
    • Investigation of drug-porous adsorbent interactions in drug mixtures with selected porous adsorbents
    • Madieh S., Simone M., Wilson W., Mehra D., and Augsburger L. Investigation of drug-porous adsorbent interactions in drug mixtures with selected porous adsorbents. J. Pharm. Sci. 96 (2007) 851-863
    • (2007) J. Pharm. Sci. , vol.96 , pp. 851-863
    • Madieh, S.1    Simone, M.2    Wilson, W.3    Mehra, D.4    Augsburger, L.5
  • 23
    • 0018868979 scopus 로고
    • Increasing dissolution rates of poorly soluble drugs by adsorption to montmorillonite
    • McGinity J.W., and Harris M.R. Increasing dissolution rates of poorly soluble drugs by adsorption to montmorillonite. Drug Dev. Ind. Pharm. 6 (1980) 35-48
    • (1980) Drug Dev. Ind. Pharm. , vol.6 , pp. 35-48
    • McGinity, J.W.1    Harris, M.R.2
  • 24
    • 0015396118 scopus 로고
    • Use of adsorbents in enhancement of drug dissolution I
    • Monkhouse D.C., and Lach J.L. Use of adsorbents in enhancement of drug dissolution I. J. Pharm. Sci. 6 (1972) 1430-1435
    • (1972) J. Pharm. Sci. , vol.6 , pp. 1430-1435
    • Monkhouse, D.C.1    Lach, J.L.2
  • 25
    • 0015395727 scopus 로고
    • Use of adsorbents in enhancement of drug dissolution II
    • Monkhouse D.C., and Lach J.L. Use of adsorbents in enhancement of drug dissolution II. J. Pharm. Sci. 6 (1972) 1435-1441
    • (1972) J. Pharm. Sci. , vol.6 , pp. 1435-1441
    • Monkhouse, D.C.1    Lach, J.L.2
  • 27
    • 84876258762 scopus 로고    scopus 로고
    • Effect of polymer on solubilization of fenofibrate by cyclodextrin complexation
    • Patel A.R., and Vavia P.R. Effect of polymer on solubilization of fenofibrate by cyclodextrin complexation. J. Inclusion Phenomena Macrocyclic Chem. 56 (2006) 247-251
    • (2006) J. Inclusion Phenomena Macrocyclic Chem. , vol.56 , pp. 247-251
    • Patel, A.R.1    Vavia, P.R.2
  • 28
    • 0017857869 scopus 로고
    • Quantative crystallinity determinations for β-lactam antibiotics by solution calorimetry: correlation with stability
    • Pikal M.J., Lukes A.L., Lang J.E., and Gaines K. Quantative crystallinity determinations for β-lactam antibiotics by solution calorimetry: correlation with stability. J. Pharm. Sci. 67 (1978) 767-773
    • (1978) J. Pharm. Sci. , vol.67 , pp. 767-773
    • Pikal, M.J.1    Lukes, A.L.2    Lang, J.E.3    Gaines, K.4
  • 29
    • 0036913259 scopus 로고    scopus 로고
    • Dissolution rate enhancement by in situ micronization of poorly water-soluble drugs
    • Rasenack N., and Muller B.W. Dissolution rate enhancement by in situ micronization of poorly water-soluble drugs. Pharm. Res. 19 (2002) 1894-1900
    • (2002) Pharm. Res. , vol.19 , pp. 1894-1900
    • Rasenack, N.1    Muller, B.W.2
  • 30
    • 0028127826 scopus 로고
    • Characterization and dissolution of fenofibrate solid dispersion systems
    • Sheu M.T., Yeh C.M., and Sokoloski T.D. Characterization and dissolution of fenofibrate solid dispersion systems. Int. J. Pharm. 103 (1994) 137-146
    • (1994) Int. J. Pharm. , vol.103 , pp. 137-146
    • Sheu, M.T.1    Yeh, C.M.2    Sokoloski, T.D.3
  • 31
    • 8744298235 scopus 로고    scopus 로고
    • Dissolution rate enhancement by adsorption of poorly soluble drugs on silica aerogels
    • Smirnova I., Suttiruengwong S., Seiler M., and Arlt W. Dissolution rate enhancement by adsorption of poorly soluble drugs on silica aerogels. Pharm. Dev. Tech. 9 (2004) 443-452
    • (2004) Pharm. Dev. Tech. , vol.9 , pp. 443-452
    • Smirnova, I.1    Suttiruengwong, S.2    Seiler, M.3    Arlt, W.4
  • 32
    • 47049108936 scopus 로고    scopus 로고
    • U.S. Department of Health and Human Services Food and Drug administration. Guidance for industry Q1A stability testing of new drug substances and products. Available via http://www.fda.gov/cder/guidance/index.htm (accessed on June 20, 2007).
    • U.S. Department of Health and Human Services Food and Drug administration. Guidance for industry Q1A stability testing of new drug substances and products. Available via http://www.fda.gov/cder/guidance/index.htm (accessed on June 20, 2007).
  • 33
    • 47049100474 scopus 로고    scopus 로고
    • U.S. Department of Health and Human Services Food and Drug administration. Guidance for industry. Dissolution testing of immediate release solid oral dosage forms. Available via http://www.fda.gov/cder/Guidance/1713bp1.pdf (accessed on June 20, 2007).
    • U.S. Department of Health and Human Services Food and Drug administration. Guidance for industry. Dissolution testing of immediate release solid oral dosage forms. Available via http://www.fda.gov/cder/Guidance/1713bp1.pdf (accessed on June 20, 2007).
  • 34
    • 47049115897 scopus 로고    scopus 로고
    • United States Pharmacopeial Convention, United States Pharmacopeial Convention Inc., USP 28, Rockville, MD p. 1088
    • United States Pharmacopeial Convention. In Vitro and In Vivo Evaluation of Dosage Forms (2005), United States Pharmacopeial Convention Inc., USP 28, Rockville, MD p. 1088
    • (2005) In Vitro and In Vivo Evaluation of Dosage Forms
  • 35
    • 37849030370 scopus 로고    scopus 로고
    • Dissolution enhancement of fenofibrate by micronization, cogrinding, and spray-drying: comparison with commercial preparations
    • Vogt M., Kunath K., and Dressman J.B. Dissolution enhancement of fenofibrate by micronization, cogrinding, and spray-drying: comparison with commercial preparations. Eur. J. Pharm. Biopharm. 68 (2008) 283-288
    • (2008) Eur. J. Pharm. Biopharm. , vol.68 , pp. 283-288
    • Vogt, M.1    Kunath, K.2    Dressman, J.B.3
  • 36
    • 29844438761 scopus 로고    scopus 로고
    • Preparation and evaluation of solid dispersions of nitrendipine prepared with fine silica particles using melt mixing method
    • Wang L., Cui F.D., and Sunada H. Preparation and evaluation of solid dispersions of nitrendipine prepared with fine silica particles using melt mixing method. Chem. Pharm. Bull. 54 (2006) 37-43
    • (2006) Chem. Pharm. Bull. , vol.54 , pp. 37-43
    • Wang, L.1    Cui, F.D.2    Sunada, H.3
  • 38
    • 0035991640 scopus 로고    scopus 로고
    • Physical stability of amorphous pharmaceuticals: importance of configurational thermodynamic quantities and molecular mobility
    • Zhou A., Zhang Geoff G.Z., Law D., Grant David J.W., and Schmitt E.A. Physical stability of amorphous pharmaceuticals: importance of configurational thermodynamic quantities and molecular mobility. J. Pharm. Sci. 1 (2002) 1863-1872
    • (2002) J. Pharm. Sci. , vol.1 , pp. 1863-1872
    • Zhou, A.1    Zhang Geoff, G.Z.2    Law, D.3    Grant David, J.W.4    Schmitt, E.A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.